ClinVar Miner

List of variants in gene HNF4A reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_175914.5(HNF4A):c.*1832G>A rs4812832 0.02019
NM_175914.5(HNF4A):c.1217-83G>A rs114265655 0.01581
NM_175914.5(HNF4A):c.225-181A>T rs111565814 0.01208
NM_175914.5(HNF4A):c.*1975G>A rs140719706 0.01125
NM_175914.5(HNF4A):c.*167T>A rs11574744 0.01097
NM_175914.5(HNF4A):c.320-243C>T rs113275885 0.01027
NM_175914.5(HNF4A):c.827-44G>C rs3212207 0.00826
NM_175914.5(HNF4A):c.1217-332A>G rs112600410 0.00818
NM_175914.5(HNF4A):c.*521G>A rs111466682 0.00755
NM_175914.5(HNF4A):c.320-100C>T rs115573889 0.00629
NM_175914.5(HNF4A):c.320-47T>C rs190319886 0.00615
NM_175914.5(HNF4A):c.320-34T>C rs112708220 0.00600
NM_175914.5(HNF4A):c.320-270A>G rs186414755 0.00598
NM_175914.5(HNF4A):c.426+166C>A rs111477514 0.00598
NM_175914.5(HNF4A):c.320-311G>T rs112439773 0.00597
NM_175914.5(HNF4A):c.426+105G>C rs111805863 0.00597
NM_175914.5(HNF4A):c.426+175G>A rs112038029 0.00597
NM_175914.5(HNF4A):c.50-216C>T rs145895048 0.00531
NM_175914.5(HNF4A):c.582+42C>T rs140376676 0.00419
NM_175914.4(HNF4A):c.-278G>A rs112444447 0.00417
NM_175914.5(HNF4A):c.1063+206C>T rs149210632 0.00417
NM_175914.5(HNF4A):c.583-27G>A rs113495257 0.00408
NM_175914.5(HNF4A):c.1063+246A>C rs73909508 0.00386
NM_175914.5(HNF4A):c.1137C>T (p.Asn379=) rs61737145 0.00384
NM_175914.5(HNF4A):c.583-77G>A rs140446007 0.00364
NM_175914.4(HNF4A):c.-401G>A rs537336047 0.00320
NM_175914.5(HNF4A):c.826+203C>T rs190584384 0.00279
NM_175914.5(HNF4A):c.744C>T (p.Asp248=) rs6031592 0.00257
NM_175914.5(HNF4A):c.84G>A (p.Ala28=) rs41282026 0.00084
NM_175914.5(HNF4A):c.426+6G>A rs182980547 0.00070
NM_175914.5(HNF4A):c.1032T>A (p.Ile344=) rs145880201 0.00062
NM_175914.5(HNF4A):c.1321A>G (p.Ile441Val) rs147638455 0.00061
NM_175914.5(HNF4A):c.138G>A (p.Thr46=) rs145845882 0.00043
NM_175914.5(HNF4A):c.726G>A (p.Val242=) rs145280017 0.00041
NM_175914.4(HNF4A):c.-129T>C rs541483698 0.00037
NM_175914.5(HNF4A):c.1176C>T (p.Asn392=) rs141448616 0.00033
NM_175914.5(HNF4A):c.582+20G>C rs370794722 0.00024
NM_175914.5(HNF4A):c.1064-19C>T rs202202465 0.00007
NM_175914.5(HNF4A):c.624C>T (p.Leu208=) rs759084238 0.00006
NM_175914.5(HNF4A):c.*1C>A rs201330472 0.00004
NM_175914.5(HNF4A):c.1017C>T (p.Phe339=) rs142268325 0.00003
NM_175914.5(HNF4A):c.50-42T>A rs550311232 0.00001
NM_175914.5(HNF4A):c.529G>A (p.Val177Ile) rs952494962 0.00001
NM_175914.5(HNF4A):c.*657G>A rs3212209
NM_175914.5(HNF4A):c.1064-19C>A rs202202465
NM_175914.5(HNF4A):c.224+17dup rs371937621
NM_175914.5(HNF4A):c.319+283TG[16] rs35406830
NM_175914.5(HNF4A):c.319+283TG[22] rs35406830

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